Okay, I figured it out.

My wife is supposed to go an oncologist for after-surgery treatment soon and we are comparing alternatives to chemotherapy! She has Stage 3C colon cancer.

I was reading lots of stuff about MMS and cancer late the other night, and came across something that talked about an alternative cancer treatment center in Colorado that used MMS as one of their therapies. I thought it was in Denver. I searched and finally found it. Turns out it was not what I remember reading. I'm not as impressed with it as I am with others I have found.

One alternative treatment center I found has given me a lot to consider. It is the Camelot Cancer Care treatment center in Tulsa, Oklahoma. I'm comparing it with another one in Scottsdale, Arizona called the Envita Medical Center.

Does anyone know anything more about either of these places?

Ryan Whitaker
Vancouver, WA

Update on my wife:

She had an emergency bowel resection done on Feb 3rd 2009 to remove an orange sized cancer. Surgery went extremely well. They found metastacized cancer in 8 of 28 lymph nodes.

We had just received our first order of MMS immediately after her surgery, and we started her on it right away. She was soon taking 10 drops twice a day with no nausea or problems. I increased it to 15 drops as an experiment. No problem. I slipped her an 18 drop dose without telling her - and that was over the limit! She spent all day with vomiting and diarrhea. I spent all day hearing what a rotten guy I am!

After that episode, we decided to put her on six doses a day, six drops each dose. She was taking them every two hours all day long. This worked out very well. She voluntarily increased the dose to seven drops each time. Worked out great.

She went to her oncologist after about three weeks of being on MMS. We printed out some information about it and gave it to her doctor. Her doctor didn't comment. However, we were very happy to find that her blood CEA count was only 3. Her doctor said they don't get excited about doing chemotherapy until the CEA count gets up past 100! So no chemotherapy is recommended at this time. They will measure her CEA count again in six months to compare.

Meanwhile my wife has increased her MMS dosage. She is taking it almost every hour now, seven drops each time. Doing well.

By the way, she is also following another anti-cancer protocal called the Budwig diet, twice a day. This is a mixture of flaxseed oil and cottage cheese. It claims a cure rate of over 90%. She has a hard time tolerating the taste of the Budwig mixture, but she is doing it anyway. She is motivated by the deaths of two of her friends from cancer in the past week. She doesn't want to end up like them!

Ryan
Vancouver, WA

I'm not positive, but I believe the Cancer Treatment Center in Oklahoma is one that Doug Kaufmann recommends. They may use the baking soda treatment I mentioned in another post. Doug has had several doctors on his show from Oklahoma and Texas who believe as he does that cancer is fungus. He is even taking phone calls now if you need to find out more info about which doctors are using this protocol. You can most likely find the number on his website if you have any questions:

Know the cause Home Page Hosted by Doug Kaufmann

Ryan, we certainly wish your wife the best. I would advise not to push too hard on the MMS. Taking every hour or two a dosage that she can continue with is more important than going higher and higher. If she gets to vomiting on it it will be very difficult to take then..slow and steady may win the race.

Personally I would rather eat the Budwig diet daily for 10 years!

Please keep us informed on her progress.

__________________
https://www.youtube.com/watch?v=WA1nw...eature=related I'd Rather Go Blind
This is not medical advice. Just opinion. Whatever you decide to do your your health is strictly your business and your choice.
Visit www.HealthSalon.org